BACITRACIN ZINC- bacitracin zinc ointment 
Blossom Pharmaceuticals

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Bacitracin Zinc Ointment

Active ingredient                         Purpose
Bacitracin Zinc 500 Units                Antibiotic

Warnings:

For external use only

Dosage & Administration

clean the affected areas
apply a small amount of product (an amount equal to the surface area of the tip of the finger) on the area 1 to 3 times daily
may be covered with a sterile bandage

Indications & Usage

  • if you are allergic to any of the ingredients
  • in the eyes
  • over large areas of the body
  • longer than 1 week unless directed by a doctor

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center right away

Purpose:

First aid to help prevent infection in:

Ask a doctor before use:


Other information

Stop Use and ask a doctor if

Inactive ingredients

Hard Paraffin, Liquid Paraffin, White Soft Paraffin

Principal Display Panel

Blossom Pharmaceuticals Bacitracin Zinc Ointment:

bacitracin zinc.jpg

Bacitracin Zinc Ointment


BACITRACIN ZINC 
bacitracin zinc ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61767-220
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
MINERAL OIL (UNII: T5L8T28FGP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61767-220-0228.35 g in 1 TUBE
2NDC:61767-220-0314.17 g in 1 TUBE
3NDC:61767-220-04113.4 g in 1 TUBE
4NDC:61767-220-07425.3 g in 1 JAR
5NDC:61767-220-050.5 g in 1 PACKET
6NDC:61767-220-010.9 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B05/14/2014
Labeler - Blossom Pharmaceuticals (677381470)
Establishment
NameAddressID/FEIBusiness Operations
Blossom Pharmaceuticals677381470manufacture(61767-220)

Revised: 5/2014
Document Id: 0b739768-64f5-4905-89aa-bb043169d94b
Set id: ebad7200-5b4b-4e5d-84db-711973412e3d
Version: 1
Effective Time: 20140514
 
Blossom Pharmaceuticals